Haque S J, Harbor P, Tabrizi M, Yi T, Williams B R
Department of Cancer Biology, The Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
J Biol Chem. 1998 Dec 18;273(51):33893-6. doi: 10.1074/jbc.273.51.33893.
Binding of interleukin (IL)-4 to its transmembrane receptor results in the Jak-mediated tyrosine phosphorylation of a number of protein components of the IL-4 signaling cascade, including Jak1, Jak2, Jak3, Tyk2, IL-4Ralpha, IRS-1, IRS-2, and Stat6 in appropriate cell types. However, the protein-tyrosine phosphatases (PTPs) that dephosphorylate these proteins and terminate signaling remained unidentified. We have noted that IL-4-dependent activation of Stat6 is sustained longer in fibroblasts than in lymphoid cells. Because Shp-1, an SH2 domain-containing PTP, is expressed primarily in hematopoietic cells, we examined whether Shp-1 activity could regulate IL-4-dependent cell signaling. Expression of an Shp-1 transgene in NIH 3T3 cells markedly reduces both IL-4-dependent Stat6 activation and Stat6-mediated transcription of IL-4-responsive genes. In accord with this, IL-4 treatment of bone marrow-derived macrophages from viable motheaten mice that express substantially reduced levels of Shp-1 activity show remarkably enhanced activation of Stat6. In addition, Stat6 activation by IL-4 is significantly enhanced in pre-B cells derived from motheaten (Shp-1 null mutant) mice compared with normal pre-B cells derived from control animals. These data clearly implicate Shp-1 in the negative regulation of the IL-4/IL-13-activated Jak-Stat pathway.
白细胞介素(IL)-4与其跨膜受体结合,会导致Jak介导的IL-4信号级联反应中一些蛋白质成分发生酪氨酸磷酸化,这些蛋白质成分包括Jak1、Jak2、Jak3、Tyk2、IL-4Rα、IRS-1、IRS-2以及特定细胞类型中的Stat6。然而,使这些蛋白质去磷酸化并终止信号传导的蛋白质酪氨酸磷酸酶(PTP)仍未明确。我们注意到,与淋巴细胞相比,成纤维细胞中Stat6的IL-4依赖性激活持续时间更长。由于含SH2结构域的PTP——Shp-1主要在造血细胞中表达,我们研究了Shp-1活性是否能调节IL-4依赖性细胞信号传导。在NIH 3T3细胞中表达Shp-1转基因,会显著降低IL-4依赖性Stat6激活以及Stat6介导的IL-4反应性基因转录。与此一致的是,用IL-4处理来自活的motheaten小鼠的骨髓来源巨噬细胞(这些巨噬细胞中Shp-1活性水平大幅降低),会显示出Stat6的激活显著增强。此外,与来自对照动物的正常前B细胞相比,来自motheaten(Shp-1基因敲除突变体)小鼠的前B细胞中,IL-4对Stat6的激活显著增强。这些数据清楚地表明Shp-1参与了IL-4/IL-13激活的Jak-Stat途径的负调控。